FDA.reportPublic FDA data

Brush Buddies ® ADVANCED WHITENING ANTI-CAVITY FLUORIDE TOOTHPASTE

Manufacturer
Ashtel Studios, Inc.
Effective date
2026-10-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-10-20 03:02:39

Label at a glance#

ProductBrush Buddies ADVANCED WHITENING ANTI-CAVITY FLUORIDE PEPPERMINT
Active ingredientSODIUM FLUORIDE
Label structure9 sections

Indications and uses

helps in the prevention of dental decay

Dosage and administration

• Do not swallow • Supervise children as necessary until capable of using without supervision • Adult and children 2 years and older    brush teeth thoroughly after meals or at least twice a day, or use as directed by a dentist or physician • Children under 6 years    instruct in good brushing and rinsing habits (to minimize swallowing) • Children under 2 years    ask a dentist or physician

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Sodium Fluoride 0.24% (0.17% w/v Fluoride ion)

Purpose

OTC - PURPOSE SECTION

Anticavity

Uses

INDICATIONS & USAGE SECTION

helps in the prevention of dental decay

Warnings

WARNINGS SECTION

Do not use if you are allergic to any of the ingredients.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children under 6 years of age.
If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• Do not swallow

• Supervise children as necessary until capable of using without supervision

• Adult and children 2 years and older
   brush teeth thoroughly after meals or at least twice a day, or use as directed by a dentist or physician

• Children under 6 years
   instruct in good brushing and rinsing habits (to minimize swallowing)

• Children under 2 years
   ask a dentist or physician

Inactive ingredients

INACTIVE INGREDIENT SECTION

Calcium Carbonate, Aqua (Water), Sorbitol, Silica, Sodium Lauryl Sulfate, Flavor, Sodium Bicarbonate, Benzyl Alcohol, PEG-8, Cellulose Gum, Xanthan Gum, Sodium Saccharin, Sodium Benzoate, Titanium Dioxide, Sodium Silicate

Questions or comments?

OTC - QUESTIONS SECTION

Call toll free 1-877-274-8358

SPL UNCLASSIFIED SECTION

• HELPS FIGHT CAVITIES

• GENTLY CLEANS TEETH

• CLEAN FRESH BREATH

• STRENGTHEN ENAMEL

• REMOVES STAINS & PLAQUE

WWW.BRUSHBUDDIES.COM
1-909-434-0911 INTERNATIONAL
PATENTS, COPYRIGHTS & TRADEMARKS GRANTED OR PENDING WORLDWIDE
DISTRIBUTED BY ASHTEL STUDIOS INC. ONTARIO, CALIFORNIA 91761

DESIGNED IN USA • MADE IN INDIA

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BB-ADVANCED WHITENING TOOTHPASTEBB-ADVANCED WHITENING TOOTHPASTE

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
c6f86816-7da6-43ea-8c25-ac9758311cc5Product name120220118
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
252e11b6-1a9a-4283-a242-df2c129c496dProduct name320170717
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316
6084a4f4-5437-c9a5-caec-5361ee075a59Product name120140508
90c5639a-61b0-88d6-ddcf-21888e94869aProduct name120140508
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877Product name120140508
9869efd7-d6dd-0665-5b67-53adbe6ef15eProduct name120140508

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
70108-20570108-205-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Name, UNII, Kind table
NameUNIIKind
SODIUM FLUORIDE8ZYQ1474W7ACTIB
CALCIUM CARBONATEH0G9379FGKIACT
WATER059QF0KO0RIACT
SORBITOL506T60A25RIACT
SILICON DIOXIDEETJ7Z6XBU4IACT
SODIUM LAURYL SULFATE368GB5141JIACT
SODIUM BICARBONATE8MDF5V39QOIACT
BENZYL ALCOHOLLKG8494WBHIACT
POLYETHYLENE GLYCOL 400B697894SGQIACT
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIEDK679OBS311IACT
XANTHAN GUMTTV12P4NEEIACT
SACCHARIN SODIUMSB8ZUX40TYIACT
SODIUM BENZOATEOJ245FE5EUIACT
TITANIUM DIOXIDE15FIX9V2JPIACT
SODIUM SILICATEIJF18F77L3IACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-07-01full-release2026-06-01 01:06:33

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
b504a623-5511-46ca-aba7-c2aa99a600cf13dba3ce-88a8-490c-a906-cfd206d1d2902025-07-01WarningsExact identifier
spl set id: 13dba3ce-88a8-490c-a906-cfd206d1d290

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.